Skip to main content

Research Repository

Advanced Search

All Outputs (3)

2,2‐Difluoroethylation of Heteroatom Nucleophiles via a Hypervalent Iodine Strategy (2024)
Journal Article
Das, S., McIvor, C., Greener, A., Suwita, C., Argent, S. P., & O'Duill, M. L. (2024). 2,2‐Difluoroethylation of Heteroatom Nucleophiles via a Hypervalent Iodine Strategy. Angewandte Chemie, https://doi.org/10.1002/anie.202410954

The 2,2-difluoroethyl group is an important lipophilic hydrogen bond donor in medicinal chemistry, but its incorporation into small molecules is often challenging. Herein, we demonstrate electrophilic 2,2-difluoroethylation of thiol, amine and alcoho... Read More about 2,2‐Difluoroethylation of Heteroatom Nucleophiles via a Hypervalent Iodine Strategy.

The properties of AGN in dwarf galaxies identified via SED fitting (2024)
Journal Article
Bichang’a, B., Kaviraj, S., Lazar, I., Jackson, R. A., Das, S., Smith, D. J., Watkins, A. E., & Martin, G. (2024). The properties of AGN in dwarf galaxies identified via SED fitting. Monthly Notices of the Royal Astronomical Society, 532(1), 613-621. https://doi.org/10.1093/mnras/stae1441

Given their dominance of the galaxy number density, dwarf galaxies are central to our understanding of galaxy formation. While the incidence of active galactic nuclei (AGN) and their impact on galaxy evolution have been extensively studied in massive... Read More about The properties of AGN in dwarf galaxies identified via SED fitting.

2,2-Difluoroethylation of heteroatom nucleophiles via a hypervalent iodine strategy (2024)
Preprint / Working Paper
Das, S., McIvor, C., Greener, A., Suwita, C., Argent, S., & O'Duill, M. 2,2-Difluoroethylation of heteroatom nucleophiles via a hypervalent iodine strategy

The 2,2-difluoroethyl group is an important lipophilic hydrogen bond donor in medicinal chemistry, but its incorporation into small molecules is often challenging. Herein, we demonstrate electrophilic 2,2 difluoroethylation of thiol, amine and alcoho... Read More about 2,2-Difluoroethylation of heteroatom nucleophiles via a hypervalent iodine strategy.